Amyotrophic Lateral Sclerosis (ALS)

Symptoms usually do not develop until after age 50, but they can start in younger people. People diagnosed with ALS have a loss of muscle strength and coordination that eventually gets worse and makes it impossible for them to do routine tasks such as going up steps, getting out of a chair, or swallowing.

Weakness can first affect the arms or legs, or the ability to breathe or swallow. As the disease gets worse, more muscle groups develop problems.

ALS does not affect the senses (sight, smell, taste, hearing, touch). Most people are able to think normally, although a small number develop dementia, causing problems with memory.

Muscle weakness starts in one body part, such as the arm or hand, and slowly gets worse until it leads to the following:

• Difficulty lifting, climbing stairs and walking
• Difficulty breathing
• Difficulty swallowing — choking easily, drooling or gagging
• Head drop due to weakness of the neck muscles
• Speech problems, such as a slow or abnormal speech pattern (slurring of words)
• Voice changes, hoarseness
• Depression
• Muscle cramps
• Muscle stiffness, called spasticity
• Muscle contractions, called fasciculations
• Muscle contractions
• Weight loss

During your visit, one of our neurologists will examine you and ask about your medical history and symptoms.

The physical exam may show:

• Weakness, often beginning in one area
• Muscle tremors, spasms, twitching, or loss of muscle tissue
• Twitching of the tongue (common)
• Abnormal reflexes
• Stiff or clumsy walk
• Decreased or increased reflexes at the joints
• Difficulty controlling crying or laughing (sometimes called emotional incontinence)
• Loss of gag reflex

Tests that may be done include:

• Blood tests to rule out other conditions
• Breathing test to see if lung muscles are affected
• Cervical spine CT or MRI to be sure there is no disease or injury to the neck, which can mimic ALS
• Electromyography to see which nerves or muscles do not work properly
• Genetic testing, if there is a family history of ALS
• Head CT or MRI to rule out other conditions
• Swallowing studies
• Spinal tap (lumbar puncture)

There is no known cure for ALS. Two medicines are available that help slow the progression of symptoms and may help people live slightly longer:

• Riluzole (Rilutek)
• Edaravone (Radicava)

Treatments to control other symptoms include:

• Baclofen or diazepam for spasticity that interferes with daily activities
• Trihexyphenidyl or amitriptyline for people with problems swallowing their own saliva

Physical therapy, rehabilitation, use of braces or a wheelchair, or other measures may be needed to help with muscle function and general health.

People with ALS tend to lose weight. The illness itself increases the need for food and calories. At the same time, problems with choking and swallowing make it hard to eat enough. To help with feeding, a tube may be placed into the stomach. A dietitian who specializes in ALS can give advice on healthy eating.

Breathing devices include machines that are used only at night, and constant mechanical ventilation.

Medicine for depression may be needed if a person with ALS is feeling sad. They also should discuss their wishes regarding artificial ventilation with their families and providers.

Over time, people with ALS lose the ability to function and care for themselves. Death often occurs within 3 to 5 years of diagnosis. About 1 in 4 people survive for more than 5 years after diagnosis. Some people live much longer, but they typically need help breathing from a ventilator or other device.

Complications of ALS include:

• Breathing in food or fluid (aspiration)
• Loss of ability to care for self
• Lung failure
• Pneumonia

Call your provider if:

• You have symptoms of ALS, particularly if you have a family history of the disorder
• You or someone else has been diagnosed with ALS and symptoms get worse or new symptoms develop
• Increased difficulty swallowing, difficulty breathing, and episodes of apnea are symptoms that require immediate attention.